JP2013537857A - 硬化性樹脂組成物及びそれを使用して製造される多層積層体 - Google Patents
硬化性樹脂組成物及びそれを使用して製造される多層積層体 Download PDFInfo
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- JP2013537857A JP2013537857A JP2013528172A JP2013528172A JP2013537857A JP 2013537857 A JP2013537857 A JP 2013537857A JP 2013528172 A JP2013528172 A JP 2013528172A JP 2013528172 A JP2013528172 A JP 2013528172A JP 2013537857 A JP2013537857 A JP 2013537857A
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- curable resin
- acrylate
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- 239000011342 resin composition Substances 0.000 title claims abstract description 83
- 239000010410 layer Substances 0.000 claims abstract description 77
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims abstract description 74
- 239000011347 resin Substances 0.000 claims abstract description 72
- 229920005989 resin Polymers 0.000 claims abstract description 72
- 239000011247 coating layer Substances 0.000 claims abstract description 71
- 239000000758 substrate Substances 0.000 claims abstract description 53
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 43
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 38
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 38
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 33
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 claims abstract description 27
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims abstract description 26
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 7
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 60
- 239000000945 filler Substances 0.000 claims description 24
- 239000002105 nanoparticle Substances 0.000 claims description 24
- 239000000377 silicon dioxide Substances 0.000 claims description 24
- 238000005299 abrasion Methods 0.000 claims description 23
- 239000004925 Acrylic resin Substances 0.000 claims description 21
- 229920000178 Acrylic resin Polymers 0.000 claims description 21
- 238000003847 radiation curing Methods 0.000 claims description 20
- 238000013007 heat curing Methods 0.000 claims description 10
- 239000004417 polycarbonate Substances 0.000 claims description 10
- 229920000515 polycarbonate Polymers 0.000 claims description 10
- 229920001187 thermosetting polymer Polymers 0.000 claims description 8
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 239000000463 material Substances 0.000 abstract description 5
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- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 15
- 125000004432 carbon atom Chemical group C* 0.000 description 15
- 230000001681 protective effect Effects 0.000 description 14
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 12
- 125000002723 alicyclic group Chemical group 0.000 description 12
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 12
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- 125000001424 substituent group Chemical group 0.000 description 12
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- 125000003118 aryl group Chemical group 0.000 description 11
- 230000000052 comparative effect Effects 0.000 description 11
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- 125000001931 aliphatic group Chemical group 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 238000007639 printing Methods 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 5
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- 125000000217 alkyl group Chemical group 0.000 description 5
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- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 5
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- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 4
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 4
- 229910052753 mercury Inorganic materials 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 238000001029 thermal curing Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
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- 239000002202 Polyethylene glycol Substances 0.000 description 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 3
- MPIAGWXWVAHQBB-UHFFFAOYSA-N [3-prop-2-enoyloxy-2-[[3-prop-2-enoyloxy-2,2-bis(prop-2-enoyloxymethyl)propoxy]methyl]-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(COC(=O)C=C)(COC(=O)C=C)COCC(COC(=O)C=C)(COC(=O)C=C)COC(=O)C=C MPIAGWXWVAHQBB-UHFFFAOYSA-N 0.000 description 3
- FHLPGTXWCFQMIU-UHFFFAOYSA-N [4-[2-(4-prop-2-enoyloxyphenyl)propan-2-yl]phenyl] prop-2-enoate Chemical class C=1C=C(OC(=O)C=C)C=CC=1C(C)(C)C1=CC=C(OC(=O)C=C)C=C1 FHLPGTXWCFQMIU-UHFFFAOYSA-N 0.000 description 3
- 239000000853 adhesive Substances 0.000 description 3
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- 239000002390 adhesive tape Substances 0.000 description 3
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 description 3
- 150000002430 hydrocarbons Chemical group 0.000 description 3
- 238000003754 machining Methods 0.000 description 3
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- 229920001223 polyethylene glycol Polymers 0.000 description 3
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical group C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 2
- MYWOJODOMFBVCB-UHFFFAOYSA-N 1,2,6-trimethylphenanthrene Chemical compound CC1=CC=C2C3=CC(C)=CC=C3C=CC2=C1C MYWOJODOMFBVCB-UHFFFAOYSA-N 0.000 description 2
- XFCMNSHQOZQILR-UHFFFAOYSA-N 2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOC(=O)C(C)=C XFCMNSHQOZQILR-UHFFFAOYSA-N 0.000 description 2
- XMLYCEVDHLAQEL-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-phenylpropan-1-one Chemical compound CC(C)(O)C(=O)C1=CC=CC=C1 XMLYCEVDHLAQEL-UHFFFAOYSA-N 0.000 description 2
- LWRBVKNFOYUCNP-UHFFFAOYSA-N 2-methyl-1-(4-methylsulfanylphenyl)-2-morpholin-4-ylpropan-1-one Chemical compound C1=CC(SC)=CC=C1C(=O)C(C)(C)N1CCOCC1 LWRBVKNFOYUCNP-UHFFFAOYSA-N 0.000 description 2
- UPTHZKIDNHJFKQ-UHFFFAOYSA-N 2-methylprop-2-enoic acid;propane-1,2,3-triol Chemical compound CC(=C)C(O)=O.CC(=C)C(O)=O.OCC(O)CO UPTHZKIDNHJFKQ-UHFFFAOYSA-N 0.000 description 2
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- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
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- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
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- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
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- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
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- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/046—Forming abrasion-resistant coatings; Forming surface-hardening coatings
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
- C09D133/04—Homopolymers or copolymers of esters
- C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
- C09D175/14—Polyurethanes having carbon-to-carbon unsaturated bonds
- C09D175/16—Polyurethanes having carbon-to-carbon unsaturated bonds having terminal carbon-to-carbon unsaturated bonds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
- C09D4/06—Organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond in combination with a macromolecular compound other than an unsaturated polymer of groups C09D159/00 - C09D187/00
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/26—Esters containing oxygen in addition to the carboxy oxygen
- C08F220/28—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety
- C08F220/281—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety and containing only one oxygen, e.g. furfuryl (meth)acrylate or 2-methoxyethyl (meth)acrylate
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2333/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
- C08J2333/04—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters
- C08J2333/06—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters of esters containing only carbon, hydrogen, and oxygen, the oxygen atom being present only as part of the carboxyl radical
- C08J2333/10—Homopolymers or copolymers of methacrylic acid esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0025—Crosslinking or vulcanising agents; including accelerators
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31507—Of polycarbonate
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
- Y10T428/31573—Next to addition polymer of ethylenically unsaturated monomer
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Laminated Bodies (AREA)
- Paints Or Removers (AREA)
- Polyurethanes Or Polyureas (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/US2010/047974 WO2012033483A1 (en) | 2010-09-07 | 2010-09-07 | Curable resin composition and multi-layer laminate manufactured using the same |
Publications (2)
| Publication Number | Publication Date |
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| JP2013537857A true JP2013537857A (ja) | 2013-10-07 |
| JP2013537857A5 JP2013537857A5 (enExample) | 2013-11-14 |
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Country Status (5)
| Country | Link |
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| US (1) | US20130164541A1 (enExample) |
| JP (1) | JP2013537857A (enExample) |
| KR (1) | KR20130131320A (enExample) |
| CN (1) | CN103080252A (enExample) |
| WO (1) | WO2012033483A1 (enExample) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2016021545A1 (ja) * | 2014-08-06 | 2016-02-11 | 三菱樹脂株式会社 | 塗布フィルム |
| JP2016037046A (ja) * | 2014-08-06 | 2016-03-22 | 三菱樹脂株式会社 | 積層ポリエステルフィルム |
| JP2016069588A (ja) * | 2014-10-01 | 2016-05-09 | 三菱樹脂株式会社 | 積層ポリエステルフィルム |
| JP2019123165A (ja) * | 2018-01-17 | 2019-07-25 | 凸版印刷株式会社 | 化粧シート、化粧材、化粧シートの製造方法 |
| JPWO2022118745A1 (enExample) * | 2020-12-04 | 2022-06-09 |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10011734B2 (en) * | 2012-02-25 | 2018-07-03 | Mitsubishi Chemical Corporation | Coated film |
| US9222130B2 (en) * | 2013-03-15 | 2015-12-29 | Keith Oxenrider | Method and apparatus for sequencing molecules |
| KR101640369B1 (ko) * | 2013-07-19 | 2016-07-22 | 배인수 | 터치스크린 패널용 커버 시트 제조방법, 이를 이용한 터치스크린 패널 제조방법 및 그에 따라 제조된 터치스크린 패널 |
| KR20150033468A (ko) * | 2013-09-24 | 2015-04-01 | 엘지이노텍 주식회사 | 터치 패널 |
| US10471655B2 (en) * | 2015-09-04 | 2019-11-12 | Carbon, Inc. | Cyanate ester dual resins for additive manufacturing |
| CN105398156B (zh) * | 2015-11-05 | 2017-12-26 | 浙江瑞欣装饰材料有限公司 | 纳米耐火板及其制作工艺 |
| JP6498146B2 (ja) | 2016-04-19 | 2019-04-10 | 富士フイルム株式会社 | 積層フィルムおよびその製造方法、偏光板、液晶パネル、液晶表示装置ならびにタッチパネル |
| CN110446760B (zh) | 2017-05-22 | 2021-12-24 | 乐金华奥斯株式会社 | 耐污染性优异的低光泽固化物及其制备方法 |
| CN108047782A (zh) * | 2017-12-13 | 2018-05-18 | 天津宝兴威科技股份有限公司 | 一种纳米银导电膜的保护涂层配方 |
| JP7054348B2 (ja) * | 2018-01-30 | 2022-04-13 | リンテック株式会社 | 粘着シート、構成体およびその製造方法 |
| CN112218753A (zh) | 2018-06-04 | 2021-01-12 | 3M创新有限公司 | 热成形耐磨多层光学膜及其制备方法 |
| KR20200133288A (ko) * | 2019-05-16 | 2020-11-27 | 삼성디스플레이 주식회사 | 고분자 수지, 이를 포함하는 윈도우 모듈, 및 이를 포함하는 표시 장치 |
| CN115151586B (zh) * | 2020-02-28 | 2024-09-20 | 卡本有限公司 | 用于增材制造的单份可湿固化树脂 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008116596A (ja) * | 2006-11-02 | 2008-05-22 | Riken Technos Corp | ハードコートフィルムおよび反射防止フィルム |
| JP2010188651A (ja) * | 2009-02-19 | 2010-09-02 | Three M Innovative Properties Co | 硬化性樹脂組成物及び当該組成物を用いて作製された多層構造体 |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4404616A1 (de) * | 1994-02-14 | 1995-08-17 | Bayer Ag | Verwendung von UV-härtbaren Beschichtungsmitteln zur Beschichtung von Polycarbonatformkörpern |
| CA2189836C (en) * | 1995-12-04 | 2004-05-25 | Angela S. Rosenberry | Coating composition and floor covering including the composition |
| EP0903363B1 (de) * | 1997-09-22 | 2005-09-28 | Basf Aktiengesellschaft | Verfahren zur Herstellung strahlungshärtbarer, Urethangruppen enthaltender Prepolymere |
| DE19741781A1 (de) * | 1997-09-22 | 1999-03-25 | Basf Ag | Verfahren zur Herstellung strahlungshärtbarer, Urethangruppen enthaltender Prepolymere |
| KR100635550B1 (ko) * | 1998-12-09 | 2006-10-18 | 니폰 가야꾸 가부시끼가이샤 | 경질 코팅물질 및 이를 포함하는 막 |
| EP1227895B1 (de) * | 1999-10-02 | 2004-11-24 | E.I. Du Pont De Nemours And Company | Verfahren zur herstellung von basislack/klarlack-zweischichtlackierungen und/oder transparenten versiegelungsschichten |
| JP4623538B2 (ja) * | 2000-06-13 | 2011-02-02 | 日本化薬株式会社 | 放射線硬化型樹脂組成物の硬化皮膜を有するフィルム |
| JP3676260B2 (ja) * | 2000-12-28 | 2005-07-27 | ナトコ株式会社 | 活性エネルギー線硬化性ウレタン(メタ)アクリレート及び活性エネルギー線硬化性組成物並びにそれらの用途 |
| JP2004010728A (ja) | 2002-06-05 | 2004-01-15 | Shinnakamura Kagaku Kogyo Kk | 紫外線硬化性組成物 |
| EP1870234A4 (en) | 2005-04-14 | 2010-09-29 | Nozomu Murata | HARDENING PLATE WITH A FINE DECORATIVE PATTERN AND METHOD FOR THE PRODUCTION THEREOF |
| CA2625455C (en) * | 2005-10-18 | 2013-06-25 | Perstorp Specialty Chemicals Ab | Dual cure composition |
| US7722955B2 (en) * | 2006-04-13 | 2010-05-25 | 3M Innovative Properties Company | Flooring substrate having a coating of a curable composition |
| US8268907B2 (en) * | 2008-06-13 | 2012-09-18 | Essilor International (Compagnie Generale D'optique) | Photocurable acrylic coating compositions having good adhesion properties to a subsequent coating and corresponding coated substrates |
-
2010
- 2010-09-07 US US13/820,819 patent/US20130164541A1/en not_active Abandoned
- 2010-09-07 CN CN2010800689423A patent/CN103080252A/zh active Pending
- 2010-09-07 KR KR1020137008523A patent/KR20130131320A/ko not_active Ceased
- 2010-09-07 WO PCT/US2010/047974 patent/WO2012033483A1/en not_active Ceased
- 2010-09-07 JP JP2013528172A patent/JP2013537857A/ja active Pending
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008116596A (ja) * | 2006-11-02 | 2008-05-22 | Riken Technos Corp | ハードコートフィルムおよび反射防止フィルム |
| JP2010188651A (ja) * | 2009-02-19 | 2010-09-02 | Three M Innovative Properties Co | 硬化性樹脂組成物及び当該組成物を用いて作製された多層構造体 |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2016021545A1 (ja) * | 2014-08-06 | 2016-02-11 | 三菱樹脂株式会社 | 塗布フィルム |
| JP2016037046A (ja) * | 2014-08-06 | 2016-03-22 | 三菱樹脂株式会社 | 積層ポリエステルフィルム |
| JP2017109499A (ja) * | 2014-08-06 | 2017-06-22 | 三菱樹脂株式会社 | 積層ポリエステルフィルム |
| KR101855877B1 (ko) | 2014-08-06 | 2018-05-09 | 미쯔비시 케미컬 주식회사 | 도포 필름 |
| US10174220B2 (en) | 2014-08-06 | 2019-01-08 | Mitsubishi Chemical Corporation | Coated film |
| JP2016069588A (ja) * | 2014-10-01 | 2016-05-09 | 三菱樹脂株式会社 | 積層ポリエステルフィルム |
| JP2019123165A (ja) * | 2018-01-17 | 2019-07-25 | 凸版印刷株式会社 | 化粧シート、化粧材、化粧シートの製造方法 |
| WO2019142822A1 (ja) * | 2018-01-17 | 2019-07-25 | 凸版印刷株式会社 | 化粧シート、化粧材、化粧シートの製造方法 |
| US11440299B2 (en) | 2018-01-17 | 2022-09-13 | Toppan Printing Co., Ltd. | Decorative sheet, decorative material, and method of producing decorative sheet |
| JPWO2022118745A1 (enExample) * | 2020-12-04 | 2022-06-09 | ||
| WO2022118745A1 (ja) * | 2020-12-04 | 2022-06-09 | 日産化学株式会社 | 液晶表示素子 |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2012033483A1 (en) | 2012-03-15 |
| US20130164541A1 (en) | 2013-06-27 |
| KR20130131320A (ko) | 2013-12-03 |
| CN103080252A (zh) | 2013-05-01 |
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